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中期因子可促进卵丘细胞和颗粒细胞在体外成熟期间增强牛卵母细胞发育能力;这可能与其抑制细胞凋亡的作用有关。

Abilities of cumulus and granulosa cells to enhance the developmental competence of bovine oocytes during in vitro maturation period are promoted by midkine; a possible implication of its apoptosis suppressing effects.

作者信息

Ikeda S, Saeki K, Imai H, Yamada M

机构信息

Laboratory of Reproductive Biology, Division of Applied Biosciences, Graduate School of Agriculture, Kyoto University, Kyoto 606-8502, Japan.

出版信息

Reproduction. 2006 Oct;132(4):549-57. doi: 10.1530/rep.1.01066.

Abstract

We previously reported that when midkine (MK), a heparin-binding growth differentiation factor was used in in vitro maturation (IVM) culture of bovine cumulus-enclosed oocytes (CEOs), their developmental competence to the blastocyst stage after in vitro fertilization (IVF) was enhanced and the effect of MK might be mediated by its action upon mural granulosa cells and cumulus cells that closely surround the oocyte. In the present study, when denuded oocytes (DOs) were matured in IVM medium with or without MK (200 ng/ml) in the presence or absence of isolated cumulus cell masses and subjected to IVF, the enhancing effects of MK on the developmental competence of DOs to the blastocyst stage after IVF were exerted only in the presence of cumulus cells. In addition, we prepared the conditioned media of granulosa cells cultured with or without 200 ng MK/ml (CMMK+ or CMMK- respectively) and examined their effects on the IVM of DOs in terms of their developmental competence to the blastocyst stage after IVF. The supplementation of CMMK+ into IVM medium at 40% (v/v) significantly enhanced the blastocyst development compared with the no additive control and the CMMK- supplemented groups. Furthermore, the effects of MK during IVM of bovine CEOs on the cumulus cell apoptosis were investigated. CEOs were cultured up to 24 h in IVM medium without (control) or with 200 ng MK/ml. The genomic DNA was extracted from CEOs at 0, 6, 12, 18 and 24 h of IVM and subjected to ligation-mediated PCR (LM-PCR) to detect the apoptotic internucleosomal DNA fragmentation. DNA fragmentation was scarcely detected at the start of IVM, whereas it increased time-dependently as the IVM culture progressed. The degree of the fragmentation was significantly lower in the MK-treatment group compared with the control group at 18 and 24 h of IVM. The apoptosis-suppressing effect of MK on cumulus cells was further confirmed in situ by using TUNEL on CEOs. In conclusion, data from the present study further confirmed that MK enhances the developmental competence of bovine oocytes via cumulus and granulosa cells. It was also demonstrated that MK suppresses the apoptosis that occurs in cumulus cells during the period of IVM of bovine CEOs. The putative soluble factor(s) from cumulus cells was suggested from the experiment using CMMK+ . MK may promote the production of such factors in part by its anti-apoptotic effects on cumulus cells.

摘要

我们之前报道过,当将肝素结合生长分化因子中期因子(MK)用于牛卵丘-卵母细胞复合体(CEO)的体外成熟(IVM)培养时,其体外受精(IVF)后发育至囊胚阶段的能力得到增强,且MK的作用可能是通过其对紧邻卵母细胞的壁颗粒细胞和卵丘细胞的作用来介导的。在本研究中,将裸卵(DO)在含有或不含有MK(200 ng/ml)的IVM培养基中,在有或没有分离的卵丘细胞团块存在的情况下进行成熟培养,然后进行IVF,结果发现MK对DO体外受精后发育至囊胚阶段能力的增强作用仅在有卵丘细胞存在时才会出现。此外,我们制备了用或不用200 ng MK/ml培养颗粒细胞的条件培养基(分别为CMMK+或CMMK-),并从DO体外受精后发育至囊胚阶段的能力方面研究了它们对DO体外成熟的影响。与无添加物对照组和添加CMMK-的组相比,在IVM培养基中添加40%(v/v)的CMMK+显著提高了囊胚发育率。此外,还研究了MK在牛CEO体外成熟过程中对卵丘细胞凋亡的影响。将CEO在不含(对照组)或含有200 ng MK/ml的IVM培养基中培养24 h。在IVM的0、6、12、18和24 h从CEO中提取基因组DNA,进行连接介导的PCR(LM-PCR)以检测凋亡的核小体间DNA片段化。在IVM开始时几乎检测不到DNA片段化,但随着IVM培养的进行,其呈时间依赖性增加。在IVM的18和24 h,MK处理组的片段化程度明显低于对照组。通过对CEO进行TUNEL原位检测,进一步证实了MK对卵丘细胞的凋亡抑制作用。总之,本研究的数据进一步证实,MK通过卵丘细胞和颗粒细胞增强牛卵母细胞的发育能力。还证明了MK抑制牛CEO体外成熟期间卵丘细胞中发生的凋亡。使用CMMK+的实验提示了来自卵丘细胞的假定可溶性因子。MK可能部分通过其对卵丘细胞的抗凋亡作用促进此类因子的产生。

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